chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103533546035335461CCAGCTACAGCGTACTTATATATAATAAATGAATAAATCTTTAAAAAAAAA1GENIChomozygous52367390
103533609735336101TATA----4GENICheterozygous51846437
103535296935352970AAT5GENIChomozygous51407443
103535642435356425CT11GENIChomozygous51846441
103535727535357276CT26GENIChomozygous51407445
103535909035359091T-16GENICheterozygous51407457
103535962335359624GA16GENICpossibly homozygous51846446
103535979235359793T-15GENIChomozygous51407459
103535987935359880AG30GENIChomozygous51407461
103536005435360055AG20GENIChomozygous51407463
103536040035360401TC18GENICpossibly homozygous51407465
103536050435360505TA25GENICpossibly homozygous51846451
103536179435361795CT25GENICpossibly homozygous51407466
103536225335362254CT22GENICpossibly homozygous51846453
103536276435362767TTT---1GENIChomozygous51407468
103536334635363349TTG---1GENIChomozygous51407474
103536349935363500CT26GENIChomozygous51407478
103536450435364505GA16GENICpossibly homozygous51846456
103536586835365869GA18GENIChomozygous51846459
103536657735366578AG15GENIChomozygous51407484
103536903935369040TTACACACACACACAC1GENIChomozygous52435317
103536931335369314GA22GENIChomozygous51407486
103536977635369777AT10GENICpossibly homozygous51846471
103537026235370263GA24GENICpossibly homozygous51846474
103537032035370321TA15GENICpossibly homozygous51846476
103537188035371881GA17GENIChomozygous51846479